| Literature DB >> 31143516 |
Wei Xie1,2,3,4, Laura Mondragón1,2,3,4, Brynjar Mauseth5,6,7, Yan Wang1,2,3,4, Jonathan Pol1,2,3,4, Sarah Lévesque1,2,3,4, Heng Zhou1,2,3,4,8, Takahiro Yamazaki9,10,11,12,13, Johannes J Eksteen14, Laurence Zitvogel9,10,11,12, Baldur Sveinbjørnsson5,15,16, Øystein Rekdal5,15,16, Oliver Kepp1,2,3,4, Guido Kroemer1,2,3,4,16,17.
Abstract
Local immunotherapies such as the intratumoral injection of oncolytic compounds aim at reinstating and enhancing systemic anticancer immune responses. LTX-315 is a first-in-class, clinically evaluated oncolytic peptide-based local immunotherapy that meets these criteria. Here, we show that LTX-401, yet another oncolytic compound designed for local immunotherapy, depicts a similar safety profile and that sequential local inoculation of LTX-401 was able to cure immunocompetent host from subcutaneous MCA205 and TC-1 cancers. Cured animals exhibited long-term immune memory effects that rendered them resistant to rechallenge with syngeneic tumors. Nevertheless, the local treatment with LTX-401 alone had only limited abscopal effects on secondary contralateral lesions. Anticancer effects resulting from single as well as sequential injections of LTX-401 were boosted in combination with PD-1 and CTLA-4 immune checkpoint blockade (ICB), and sequential LTX-401 treatment combined with double ICB exhibited strong abscopal antineoplastic effects on contralateral tumors underlining the potency of this combination therapy.Entities:
Keywords: Oncolysis; anticancer therapy; checkpoint blockade; immunogenic cell death
Year: 2019 PMID: 31143516 PMCID: PMC6527292 DOI: 10.1080/2162402X.2019.1594555
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110